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rs886043086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome14
Position21395036
GeneCHD8
is asnp
is mentioned by
dbSNPrs886043086
dbSNP (classic)rs886043086
ClinGenrs886043086
ebirs886043086
HLIrs886043086
Exacrs886043086
Gnomadrs886043086
Varsomers886043086
LitVarrs886043086
Maprs886043086
PheGenIrs886043086
Biobankrs886043086
1000 genomesrs886043086
hgdprs886043086
ensemblrs886043086
geneviewrs886043086
scholarrs886043086
googlers886043086
pharmgkbrs886043086
gwascentralrs886043086
openSNPrs886043086
23andMers886043086
23andMe allrs886043086
SNPshotrs886043086
SNPdbers886043086
MSV3drs886043086
GWAS Ctlgrs886043086
Max Magnitude0
ClinVar
Risk rs886043086(A;A)
Alt rs886043086(A;A)
Reference Rs886043086(-;-)
Significance Pathogenic
Disease Autism
Variation info
Gene CHD8
CLNDBN Autism, susceptibility to, 18
Reversed 0
HGVS NC_000014.8:g.21863195dupA
CLNSRC
CLNACC RCV000313270.1,